High-coverage nanopore sequencing of samples from the 1000 Genomes Project to build a comprehensive catalog of human genetic variation

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Figure 1.
Figure 1.

Summary statistics of samples, sequencing, and small variant detection. (A) Samples selected for sequencing are shown by superpopulation and sex. (B) Violin plots showing average read length, read N50, and average depth of coverage for all 100 samples. (C) DNA was extracted from cells grown from aliquots received from Coriell and sequenced using the R9.4.1 pore. Data were analyzed using both alignment- and assembly-based approaches.

This Article

  1. Genome Res. 34: 2061-2073

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